Charge carrier mobility and concentration as a function of composition in AgPO3-AgI glasses

Conductivity data of the xAgI(1 - x)AgPO(3) system (0 ≤ x ≤ 0.5) were collected in the liquid and glassy states. The difference in the dependence of ionic conductivity on temperature below and above their glass transition temperatures (T(g)) is interpreted by a discontinuity in the charge carrier's mobility mechanisms. Charge carrier displacement occurs through an activated mechanism below T(g) and through a Vogel-Fulcher-Tammann-Hesse mechanism above this temperature. Fitting conductivity data with the proposed model allows one to determine separately the enthalpies of charge carrier formation and migration. For the five investigated compositions, the enthalpy of charge carrier formation is found to decrease, with x, from 0.86 to 0.2 eV, while the migration enthalpy remains constant at ≈0.14 eV. Based on these values, the charge carrier mobility and concentration in the glassy state can then be calculated. Mobility values at room temperature (≈10(-4) cm(2) V(-1) s(-1)) do not vary significantly with the AgI content and are in good agreement with those previously measured by the Hall-effect technique. The observed increase in ionic conductivity with x would thus only be due to an increase in the effective charge carrier concentration. Considering AgI as a weak electrolyte, the change in the effective charge carrier concentration is justified and is correlated to the partial free energy of silver iodide forming a regular solution with AgPO(3).     

Heat conduction across molecular junctions between nanoparticles

We investigate the problem of heat conduction across molecular junctions connecting two nanoparticles, both in vacuum and in a liquid environment, using classical molecular dynamics simulations. In vacuum, the well-known result of a length independent conductance is recovered; its precise value, however, is found to depend sensitively on the overlap between the vibrational spectrum of the junction and the density of states of the nanoparticles that act as thermal contacts. In a liquid environment, the conductance is constant up to a crossover length, above which a standard Fourier regime is recovered.     

Fitting models to correlated data III: A comparison between residual analysis and other methods

Applications of the χ² test, the F test, the Durbin-Watson d test, and the f (or Sign) test, to examples of correlated data treatment, show important drawbacks with the d test and (apparently) with the f test. An analytical approach based on residual analysis suggests an improvement in their use that leads to better results at lowest order; it also points out a distinction between goodness-of-fit tests, as the f test, and goodness-of-modeling tests, as the χ² and F tests. The residual analysis method is applied to the same examples; it looks faster, simpler, and often more accurate than the classical ones.     

Thermal stability of spin valve sensors using artificial Co/Ir based ferrimagnets

Hard-soft spin valve structures have been grown by molecular beam epitaxy on MgO(0 0 1) substrates. The hard magnetic layer consists of an artificial Co/Ir/Co ferrimagnet system (AFi), while a Fe/Co bilayer from the buffer has been used as a soft detection layer. The Fe layer has been grown at 600°C giving rise to a monocrystalline layer with a BCC structure. Consequently, this layer presents a hard and a easy magnetization axis, respectively, along the BCC [1 1 0] and the [1 0 0] directions. The AFi system presents dramatic differences after successive annealing steps up to 350°C. An increase of the GMR from 3% to 3.5% is observed after annealing at 250°C while the coercive field of the AFi and the GMR plateau are strongly reduced. After further annealing at higher temperature the GMR drops down accompanied with a strong decrease in the antiparallel alignment amount in the AFi system. Rutherford back scattering measurements have been performed to investigate the changes in the interface morphology and to correlate it to the magneto-transport properties.     

Self-organized structures in a superorganism: do ants “behave” like molecules?

While the striking structures (e.g. nest architecture, trail networks) of insect societies may seem familiar to many of us, the understanding of pattern formation still constitutes a challenging problem. Over the last two decades, self-organization has dramatically changed our view on how collective decision-making and structures may emerge out of a population of ant workers having each their own individuality as well as a limited access to information. A variety of collective behaviour spontaneously outcome from multiple interactions between nestmates, even when there is no directing influence imposed by an external template, a pacemaker or a leader. By focussing this review on foraging structures, we show that ant societies display some properties which are usually considered in physico-chemical systems, as typical signatures of self-organization. We detail the key role played by feed-back loops, fluctuations, number of interacting units and sensitivity to environmental factors in the emergence of a structured collective behaviour. Nonetheless, going beyond simple analogies with non-living self-organized patterns, we stress on the specificities of social structures made of complex living units of which the biological features have been selected throughout the evolution depending on their adaptive value. In particular, we consider the ability of each ant individual to process information about environmental and social parameters, to accordingly tune its interactions with nestmates and ultimately to determine the final pattern emerging at the collective level. We emphasize on the parsimony and simplicity of behavioural rules at the individual level which allow an efficient processing of information, energy and matter within the whole colony.     

Fast characterization of foodstuff by headspace mass spectrometry (HS-MS)

The field of the rapid characterization of products by HS-MS is reviewed. The general principle of HS-MS systems consists of introducing volatile components present in the HS of a sample without prior chromatographic separation into the ionization chamber of a mass spectrometer. The spectrum resulting from simultaneous ionization and fragmentation of the mixture of molecules introduced constitutes a “fingerprint” that is characteristic of the product being analyzed. Exploitation of this spectral information allows one determine the composition of the sample.     

New solid electrolytes based on bismuth oxide

The oxide ion conducting systems Bi₂O₃-Y₂O₃-Pr₆O₁₁ and Bi₂O₃-Y₂O₃-ZrO₂ have been prepared and studied in order to combine the advantages of stabilized Bi₂O₃ and ZrO₂ solid electrolytes. Coprecipitation of high purity oxides was used for preparation. The formation of the fluorite-type cubic structure was confirmed by X-ray powder diffraction analysis. The relative contributions of ions and electrons to the total conductivity were measured by the concentration cell method. Using Ultraviolet Photoemission Spectroscopy (UPS) we have determined the work function Φ of electrons, the position of the Fermi level in relation to the valence band edge (E_F-E_V) and the change of the ionization potential (I) as a function of temperature. For bismuth oxide-based solid electrolytes, we used an Fe/FeO mixture as reference contact to establish a defined oxygen partial pressure in the solid electrolyte sample. Oxygen isotope exchange experiments were performed in an exchange cell with a gas regulating system and mass spectrometer to determine the oxygen surface exchange rate. Paper presented at the 2nd Euroconference on Solid State Ionics, Funchal, Madeira, Portugal, Sept. 10–16, 1995     

A new preparation of samarium dibromide and its use in stoichiometric and catalytic pinacol coupling reactions

A new convenient preparation of samarium dibromide in THF is reported. Pinacol coupling reactions using SmBr₂ in catalytic amounts together with mischmetall as a coreductant have been performed with a variety of carbonyl compounds.     

Electrochemical sensors based on transition metal oxide bronzes

Tungsten and molybdenum oxide bronzes of the general formulas A_xMO₃ and A_xM₆O₁₇ (A=K, Li, Na; M=W, Mo) are well known as electrode materials with good response to pH changes. However, there is also a high cross sensitivity to other ions, e.g. Na⁺ or Li⁺. Currently, the synthesis of tailored materials for special applications is the priority task. Preparation routes such as fused salt electrolysis, solid state reactions in vacuum or hydrothermal synthesis were studied. New compounds of the general formula Li_xMo_1−yW_yO₃ and also A_xWO₃ (A = bi- or trivalent) have a high technological potential. Preliminary experiments have shown that some of these new materials possess properties of reference electrodes within a restricted pH range. To prepare electrodes, usually single crystals are required. This is adverse because of high operating expense of single crystal synthesis. In some cases it is also possible to use polycrystalline materials for the preparation. Paper presented at the 9th EuroConference on Ionics, Ixia, Rhodes, Greece, Sept. 15 – 21, 2002.